A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408346



Internal ID22466216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141204863..141211390hg38UCSC Ensembl
chr3:140923705..140930232hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg386528
hg196528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901689
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408346
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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